| NM_054012.4:c.689G=
                    
                              MANE Select | NP_446464.1:p.Gly230= | 
            
              | ENST00000352480.10:c.689G=
                    
                        MANE Select | ENSP00000253004.6:p.Gly230= | 
            
              | NM_000050.4:c.689G= | NP_000041.2:p.Gly230= | 
            
              | NM_054012.3:c.689G= | NP_446464.1:p.Gly230= | 
            
              | ENST00000352480.9:c.689G= | ENSP00000253004.6:p.Gly230= | 
            
              | ENST00000372393.7:c.689G= | ENSP00000361469.2:p.Gly230= | 
            
              | ENST00000372394.5:c.689G= | ENSP00000361471.1:p.Gly230= | 
            
              | ENST00000467695.5:n.398G= |  | 
            
              | ENST00000470849.4:n.414G= |  | 
            
              | ENST00000492400.5:n.198G= |  | 
            
              | ENST00000493984.6:n.513-47G= |  | 
            
              | XM_005272200.2:c.689G= | XP_005272257.1:p.Gly230= | 
            
              | XM_005272200.3:c.689G= | XP_005272257.1:p.Gly230= | 
            
              | XM_011518705.1:c.803G= | XP_011517007.1:p.Gly268= | 
            
              | XM_011518705.2:c.803G= | XP_011517007.1:p.Gly268= | 
            
              | XM_017014729.1:c.785G= | XP_016870218.1:p.Gly262= |